Executive - Quality Assurance

Area and line clearance for Manufacturing, Packing & Dispensing activity in production area.
- In process checks in Manufacturing and Packing activity.
- Daily verification of weighing balance calibration activity.
- Daily verification of environmental monitoring of raw material staging area and Manufacturing and Packing area.
- Verification of each equipment cleanliness and area cleanliness during line clearance
- Verification and review of online Batch Manufacturing Records.
- Issuance of BMR / BPR, logbooks, formats. Re-issuance of additional page requirement of BMR / BPR on requisition by production.
- Sampling of bulk stage, finished goods analysis and control sample.
- Verification of production documents.
- Daily nonconformance observation reported and maintained.
- In process quality checks in Tablet, Liquid, HNH, ANH manufacturing dept.
- Line Clearance for Manufacturing, Packing & Dispensing activity.
- Sampling of validation sample (Process, packaging & cleaning), rinse & swab samples.
- Review of production records and Finished Goods verification.
- On job training to the new people working in the production area.
- Statistical Process Monitoring.
- Online observation of process deviation and effective implementation of CAPA.
- Reporting of daily nonconformance.
- Execution of requirements for food/Dietary supplements regulations for export market (US)-21 CFR Part 111
- Ensuring avoidance of breach of data integrity in area.
- Implementation of effective sanitation program in area.
- Imparting required training to shop floor personnel.
- Adherence to the requirements of EHS norms.
- Execution of various initiatives as are suggested by corporate functions (SEEDS, Learning university, Quality mindset).
- Customer centricity.
- Document Archival.
- To determine internal and external QEHS issues as well as needs and expectations of relevant interested parties and monitor the same.
- To implement QEHS policy & objectives.
- To ensure participation and consultation of worker.
- Ensure use of PPE
- To identify & communicate incidents, QEHS nonconformities, investigate and take corrective actions on the same.
- To ensure work permit system during maintenance activities.
- To implement QEHS continual improvement projects at site and monitor.
- To ensure disposal of waste.
- Authorised to prevent improper workplace conditions.
- Authorised for reporting of Hazards, Incident, Accidents and Near miss reporting.
- Authorised to prepare OH&S performance document.
- Authorised to conduct training of workmen’s related to OHSMS.

In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth.

Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices.

**Equal employment opportunity**

Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics.

We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice.

**Piramal Pharma Solutions (PPS)**is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limited’s investment in Yapan Bio Private Limited. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide.